|
Viruses
|
Yes (i.e., hepatitis B, C, D viruses, EBV, CMV, HSV-1)
|
Yes (i.e., CAV-1, herpes virus, canine acidophil cell virus hepatitisa)
|
|
Microbes
|
Yes (Listeria monocytogenes, Brucella mellitensis, Legionella pneumophila, Treponema pallidum, Helicobacter hepaticus)
|
Yes (Leishmania infantum, Ehrlichia canis, Corynebacterium parvum, Bartonella, Leptospirae, Helicobacter species) [79]
|
|
Toxins and drugs
|
|
Ethanol
|
Yes
|
Non-applicable
|
|
Immunosuppressants
|
Yes
|
Yes
|
|
Anticonvulsants
|
Yes
|
Yes
|
|
Genetic diseases
|
|
Alpha-1 antitrypsin deficiency
|
Yes
|
Yes (rarely reported)b [24]
|
|
Copper storage disease
|
Yes
|
Yes
|
|
Most commonly is Wilson disease caused by mutation in a gene on chromosome 13 that encodes for a P-type ATPase
|
Caused mainly by a mutation of MURR1 gene
|
|
Rarely other types of impaired copper excretion
|
Rarely other types [28]
|
|
Metabolic diseases
|
Yes (various, well studied as haemochromatosis, porphyrias)
|
Yes (Various, less extensively studied)
|